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1-(2,6-dichlorophenyl)-N-methylmethanamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15205-19-3

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15205-19-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15205-19-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,0 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15205-19:
(7*1)+(6*5)+(5*2)+(4*0)+(3*5)+(2*1)+(1*9)=73
73 % 10 = 3
So 15205-19-3 is a valid CAS Registry Number.

15205-19-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2,6-dichlorophenyl)-N-methylmethanamine

1.2 Other means of identification

Product number -
Other names (2,6-dichloro-benzyl)-methyl-amine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:15205-19-3 SDS

15205-19-3Relevant academic research and scientific papers

DERIVATIVES OF 4-(2-AMINO-1-HYDROXIETHYL)PHENOL AS AGONISTS OF THE β2 ADRENERGIC RECEPTOR

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Page/Page column 24-25, (2008/06/13)

This invention is directed to compounds of formula (I): to pharmaceutical compositions comprising them; to combination products comprising them; and to their use in therapy.

TACHYKININ RECEPTOR ANTAGONISTS

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Page 29, (2010/02/10)

The present invention relates to selective NK-1 receptor antagonists of Formula (I) or a pharmaceutically acceptable salt thereof, for the treatment of disorders associated with an excess of tachykinins.

Benzylamines: Synthesis and evaluation of antimycobacterial properties

Meindl,Von Angerer,Schonenberger,Ruckdeschel

, p. 1111 - 1118 (2007/10/02)

The synthesis of benzylamines with various N-alkyl chains and substituents in the aromatic system as well as their evaluation on Mycobacterium tuberculosis H 37 Ra are described. The most active compounds in this test, N-methyl-3-chlorobenzylamine (MIC 10.2 μg/mL), N-methyl-3,5-dichlorobenzylamine (93, MIC 10.2 μg/mL), and N-butyl-3,5-difluorobenzylamine (MIC 6.4 μg/mL), also exhibited a marked inhibitory effect on Mycobacterium marinum and Mycobacterium lufu used for the determination of antileprotic properties. The combination of 93 with aminosalicylic acid, streptomycin, or dapsone exert marked supra-additive effects on M. tuberculosis H 37 Ra.

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